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Надежда Альбертовна Бузмакова

Observed names: Buzmakova, N. A., Buzmakova, N.A., N. A. Buzmakova
ORCID: 0000-0003-3171-0438
Observed ORCID: 0000-0003-3171-0438
OpenAlex ID: A5072926051
Structure and Analgesic Activity of 13-(N-Aryl(N,N-Diethyl)Aminocarbonyl)-9-Methyl-11-Thioxo-8-Oxa-10,12-Diazatricyclo [7.3.1.02,7]Trideca-2,4,6-Trienes and Their 10-N-Phenyl Derivatives
2018 · V. L. Gein, T. M. Zamaraeva, et al. · Pharmaceutical Chemistry Journal · 10
Synthesis and Analgesic Activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides
2016 · V. L. Gein, T. M. Zamaraeva, et al. · Pharmaceutical Chemistry Journal · 9
The Synthesis and Evaluation of Non-steroidal Antiinflammatory Activity of N,6-diaryl-4-methyl-2-thioxo-1,2,3,6-tetrahydropyrimidine-5-carboxamides
2022 · N. A. Buzmakova, I. P. Rudakova, et al. · Drug development & registration · 7
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Synthesis and Anti-Inflammatory Activity of N,6-Diaryl-4-Methyl-2-Thioxo-1,2,3,6-Tetrahydropyrimidine-5-Carboxamides
2021 · N. A. Buzmakova, I. P. Rudakova, et al. · Pharmaceutical Chemistry Journal · 5
Synthesis of N-aryl- and N,N-diethyl-9-methyl-11-sulfanylidene-8-oxa-10,12-diazatricyclo[7.3.1.02,7]trideca-2,4,6-triene-13-carboxamides
2016 · T. M. Zamaraeva, V. L. Gein, et al. · Russian Journal of Organic Chemistry · 5
Application of X-ray Fluorescence and Radiation Methods for the Analysis of Medicinal Plant Raw Materials on the Example of Achilleae millefolii herba
2023 · I. Yu. Kalikina, A. Yu. Turyshev, et al. · Drug development & registration · 3
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Structural Features and Anti-Inflammatory Activity of 13-(N-Arylaminocarbonyl)-9-Methyl-11-Thioxo-8-Oxa-10,12-Diazatricyclo-[7.3.1.02,7]Trideca-2,4,6-Trienes and Their 10-N-Phenyl-Substituted Derivatives
2023 · N. A. Buzmakova, T. M. Zamaraeva, et al. · Pharmaceutical Chemistry Journal · 3
Synthesis of N-Aryl- and N,N-diethyl-2-methyl-3-phenyl-4-sulfanylidene-3,4,5,6-tetrahydro-2H-2,6-methano-1,3,5-benzoxadiazocine-11-carboxamides
2017 · V. L. Gein, T. M. Zamaraeva, et al. · Russian Journal of Organic Chemistry · 3
Synthesis of 6-aryl-N,N-diethyl-4-methyl-2-sulfanylidene-1,2,3,6-tetrahydropyrimidine-5-carboxamides
2016 · V. L. Gein, N. A. Buzmakova, et al. · Russian Journal of Organic Chemistry · 3
Assessment of Antihypoxic Activity of S-analoges of Dihydropyrimidin-2-ones and Their Condensed Derivatives
2023 · N. A. Buzmakova, T. M. Zamaraeva, et al. · Drug development & registration · 2
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Investigation of the «Structure – analgesic activity» Relationship Using Molecular Docking for Cyclooxygenases 1 and 2 in the Series 5-N-arylaminocarbonyl-6-(get)aryl-4-methyl-1,2,3,6-tetrahydropyrimidine-2-thiones
2023 · N. A. Buzmakova, K. V. Аndryukov, et al. · Drug development & registration · 2
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Оценка острой токсичности и анальгетического действия этил 6’-амино-2-оксо-5’-циано-2’H-спиро-[индолин-3,4’-пирано[2,3-с]пиразол]-3’-карбоксилатов
2025 · А. С. Гоман, Надежда Альбертовна Бузмакова, et al. · Химико-фармацевтический журнал · 1
Evaluation of the Anti-Inflammatory Activity of N,4-diaryl-1,6-dimethyl-2-thioxo(oxo)-1,2,3,4-tetrahydropyrimidine-5-carboxamides
2025 · T. M. Zamaraeva, N. A. Buzmakova, et al. · Pharmaceutical Chemistry Journal · 1
Hepatoprotective Activity of Pine cones Extract
2023 · D. K. Gulyaev, S. S. Zykova, et al. · Drug development & registration · 1
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Study of the Anti-inflammatory Activity of 2-hydroxy-4-oxo-4-R-2-butenoates of Heterylammonium, which Have an Effect on the Blood Clotting System
2023 · F. V. Sobin, N. A. Pulina, et al. · Drug development & registration · 1
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Antimicrobial Activity of New N-substituted Amides of Aroylpyruvic Acids and Their Silver Salts
2023 · V. V. Novikova, V. O. Vasilev, et al. · Drug development & registration · 1
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Изучение структурных особенностей и противовоспалительной активности 13-(N-ариламинокарбонил)-9-метил-11-тиоксо-8-окса-10,12-диазатрицикло[7.3.1.02,7]тридека-2,4,6-триенов и их 10-N-фенилпроизводных
2022 · Надежда Альбертовна Бузмакова, Т. М. Замараева, et al. · Химико-фармацевтический журнал · 1
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Синтез и анальгетическая активность N,6-диарил-4-метил-2-тиоксо-1,2,3,6-тетрагидропиримидин-5-карбоксамидов
2016 · Владимир Леонидович Гейн, Татьяна Михайловна Замараева, et al. · Химико-фармацевтический журнал · 1
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Synthesis of N,6-diaryl-2-imino-4-methyl-3-cyano-1,2,3,6-tetrahydropyrimidine-5-carboxamides
2015 · V. L. Gein, T. M. Zamaraeva, et al. · Russian Journal of General Chemistry · 1
Evaluation of Acute Toxicity and Analgesic Activity of Diethyl 6-aryl-3,6-dihydrotetrazolo[1,5-a]-pyrimidine-4,5-dicarboxylates
2026 · A. A. Shaikhutdinova, N. A. Buzmakova, et al. · Pharmaceutical Chemistry Journal
Оценка острой токсичности и анальгетической активности диэтил 6-арил-3,6-дигидротетразоло[1,5-a]пиримидин-4,5-дикарбоксилатов
2026 · Альбина Альбертовна Шайхутдинова, Надежда Альбертовна Бузмакова, et al. · Химико-фармацевтический журнал
Structure–Activity (Antioxidant) Regression Relationship in a Model Inhibiting Fluorescence Activity of the Ecolume Strain Using Molecular Docking with Superoxide Dismutase of Substituted Benzo[4,5]Imidazo[1,2-a]Pyrimidin-2(1H)-Ones
2026 · N. A. Buzmakova, K. V. Andryukov, et al. · Pharmaceutical Chemistry Journal
Antioxidant and antiradical activity of alkyl 6´-amino-5´-cyano-2-oxo-2´H-spiro[indolin-3,4-pyrano[2,3-c]pyrazole]-3´-carboxylates
2026 · A. S. Goman, N. A. Buzmakova, et al. · Applied Information Aspects of Medicine (Prikladnye informacionnye aspekty mediciny)
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Synthesis and investigation of interaction with COX-2 methyl/ethyl 6-amino-5-cyano-2-oxo-2-phenyl-2H-spiro[indoline-3,4-pyrano[2,3-c]pyrazole]-3-carboxylates, evaluation of their analgesic activity in experiment
2026 · N. A. Buzmakova, K. V. Andryukov, et al. · Applied Information Aspects of Medicine (Prikladnye informacionnye aspekty mediciny)
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Исследование регрессионной зависимости «структура — антиоксидантная активность» на модели ингибирования флуоресцентной активности штамма «Эколюм» с использованием молекулярного докинга по супероксиддисмутазе замещенных бензо[4,5]имидазо[1,2-a]пиримидин-2(1H)-онов
2026 · Надежда Альбертовна Бузмакова, Константин Вячеславович Андрюков, et al. · Химико-фармацевтический журнал
Works count: 46
Citation count: 60
H-index: 5
I10-index: 1
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